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created at |
2024-09-23 16:23:50 UTC |
updated at |
2024-09-23 18:22:39 UTC |
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Terms for rare diseases as defined in ORDO.
The entries were initially sourced from the ORDO version 2024-07-03 as stored in BioPortal.
Namespace: http://www.orpha.net/ORDO/
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20,514 entries
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There is 0 pattern entry.
CDG-IIm
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Orphanet_356961 |
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CDG2M
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Orphanet_356961 |
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COXPD
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Orphanet_35696 |
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SLC35A2-CDG
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Orphanet_356961 |
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Combined OXPHOS defect
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Orphanet_35696 |
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Combined OXPHOS deficiency
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Orphanet_35696 |
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Congenital disorder of glycosylation type 2m
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Orphanet_356961 |
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Congenital disorder of glycosylation type IIm
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Orphanet_356961 |
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Combined oxidative phosphorylation defect
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Orphanet_35696 |
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CDG syndrome type IIm
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Orphanet_356961 |
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